A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance

פריטים דומים

• Connexin46 mutations in autosomal dominant congenital cataract.
  מאת: Mackay, D, et al.
  יצא לאור: (1999)
• Investigation of crystallin genes in familial cataract, and report of two disease associated mutations
  מאת: Burdon, K, et al.
  יצא לאור: (2004)
• The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes
  מאת: McKay, J D, et al.
  יצא לאור: (2005)
• A novel mutation in the GJA3 (connexin46) gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family
  מאת: Yang, Guoxing, et al.
  יצא לאור: (2011)
• Two novel mutations of connexin genes in Chinese families with autosomal dominant congenital nuclear cataract
  מאת: Ma, Z, et al.
  יצא לאור: (2005)